CA1224489A - Deodorisation process for triglyceride oil - Google Patents
Deodorisation process for triglyceride oilInfo
- Publication number
- CA1224489A CA1224489A CA000454958A CA454958A CA1224489A CA 1224489 A CA1224489 A CA 1224489A CA 000454958 A CA000454958 A CA 000454958A CA 454958 A CA454958 A CA 454958A CA 1224489 A CA1224489 A CA 1224489A
- Authority
- CA
- Canada
- Prior art keywords
- oil
- condenser
- flow path
- process according
- vapour phase
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000000034 method Methods 0.000 title claims abstract description 32
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 239000000463 material Substances 0.000 claims abstract description 18
- 230000007935 neutral effect Effects 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 239000012071 phase Substances 0.000 claims description 53
- 230000007423 decrease Effects 0.000 claims description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000007790 solid phase Substances 0.000 claims description 4
- 239000007791 liquid phase Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 abstract description 12
- 239000003921 oil Substances 0.000 description 61
- 235000019198 oils Nutrition 0.000 description 61
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000839 emulsion Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 7
- 235000010469 Glycine max Nutrition 0.000 description 7
- 238000006386 neutralization reaction Methods 0.000 description 7
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 239000003240 coconut oil Substances 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 235000021588 free fatty acids Nutrition 0.000 description 4
- 235000019484 Rapeseed oil Nutrition 0.000 description 3
- 235000019486 Sunflower oil Nutrition 0.000 description 3
- 238000010924 continuous production Methods 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 239000002600 sunflower oil Substances 0.000 description 3
- 229930003799 tocopherol Natural products 0.000 description 3
- 239000011732 tocopherol Substances 0.000 description 3
- 235000019149 tocopherols Nutrition 0.000 description 3
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 3
- 235000019482 Palm oil Nutrition 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000010923 batch production Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000021323 fish oil Nutrition 0.000 description 2
- 239000002540 palm oil Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
- B01D5/0033—Other features
- B01D5/0036—Multiple-effect condensation; Fractional condensation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
- B01D5/0003—Condensation of vapours; Recovering volatile solvents by condensation by using heat-exchange surfaces for indirect contact between gases or vapours and the cooling medium
- B01D5/0012—Vertical tubes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B1/00—Production of fats or fatty oils from raw materials
- C11B1/10—Production of fats or fatty oils from raw materials by extracting
- C11B1/108—Production of fats or fatty oils from raw materials by extracting after-treatment, e.g. of miscellae
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/12—Refining fats or fatty oils by distillation
- C11B3/14—Refining fats or fatty oils by distillation with the use of indifferent gases or vapours, e.g. steam
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S203/00—Distillation: processes, separatory
- Y10S203/22—Accessories
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Microbiology (AREA)
- Fats And Perfumes (AREA)
- Engine Equipment That Uses Special Cycles (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
Deodorisation process for triglyceride oil Process and apparatus for deodorising triglyceride oil comprises passing dry steam through the oil, the oil being at a temperature between 160 and 280°C and under a pressure of between 0.1 to 8.0 mbar and condensing by indirect condenser means a vapour phase having a Reynolds number less than 2300 and comprising steam, volatile materials from the oil and less than 100 mg neutral oil per m3 of steam when measured under the conditions prevailing in the headspace above the oil. The condensate can be solid or liquid form. In either case the condensate can be readily drained from the condenser.
Deodorisation process for triglyceride oil Process and apparatus for deodorising triglyceride oil comprises passing dry steam through the oil, the oil being at a temperature between 160 and 280°C and under a pressure of between 0.1 to 8.0 mbar and condensing by indirect condenser means a vapour phase having a Reynolds number less than 2300 and comprising steam, volatile materials from the oil and less than 100 mg neutral oil per m3 of steam when measured under the conditions prevailing in the headspace above the oil. The condensate can be solid or liquid form. In either case the condensate can be readily drained from the condenser.
Description
- 1 - A.420 DEODORISATION PROCESS FOR TRIGLYCERIDE OIL
The present invention relates to a process for deodorising triglyceride oil.
s Traditionally deodorisation of triglyceride oil involves heating the oil under low pressure and passing through steam which entrains objectionable volatile substances and other material. The treated oil is cooled and is available for further processing. The steam and entrained distillation vapours are condensed and either disposed of or valuable materials extracted from the distillate prior to disposal. Conventionally condensation oc~urs by direct contact with water. To effeot condensation and removal of distillate from the condenser large amounts of water are required which can cause problPms in disposing of the effluent formed.
One approach to overcome the effluent disposal problem is to use indirect surface condensers. Their use however in the past has on the whole been deliberately avoided as the condensate of water and entrained materials is well known to form an intractable emulsion which not only proved very difficulty to clean from the condenser ~zz~
- ~ - A.420 suxface, but as it built up steadily reduced the efficacy of the condenser. One attempt to provide a process involving the use of a surface condenser which allegedly avoided the problems associated with the condensate emulsion is described in DE-A-29 38 805 which teaches condensing the steam and entrained materials at a temperature above 30C and relatively high pressures requiring higher energy input. An alternative approach to the problem is advocated in GB- A-l 080 057 which employs an indirect freezer condenser operating at a temperature between ~20 and -40C so that the condensate forms in the solid phase. In practice however we have found that in use each of these process~s as described gives rise to one or more problems.
According to the present invention there is provided a process for deodorising a triglyceride oil comprising passing dry steam throu~h the oil, the oil being at a temperature between 160C and 280C and under a pressure of between 0.1 to 8.0 mbar and condensing by indirect condenser means a vapour phase having a Reynolds number below 2300 and comprising steam, volatile materials from the oil and less than 100 mg neutral oil per m3 of steam when measured under the conditions prevailing in the headspace above the oil.
We have discovered that the combination of the use of dry steam, low headspace pressures in the range 0.1 to 8.0 mbax, preferably 0.1 to 4.0 mbar, more preferably 0.5 to
The present invention relates to a process for deodorising triglyceride oil.
s Traditionally deodorisation of triglyceride oil involves heating the oil under low pressure and passing through steam which entrains objectionable volatile substances and other material. The treated oil is cooled and is available for further processing. The steam and entrained distillation vapours are condensed and either disposed of or valuable materials extracted from the distillate prior to disposal. Conventionally condensation oc~urs by direct contact with water. To effeot condensation and removal of distillate from the condenser large amounts of water are required which can cause problPms in disposing of the effluent formed.
One approach to overcome the effluent disposal problem is to use indirect surface condensers. Their use however in the past has on the whole been deliberately avoided as the condensate of water and entrained materials is well known to form an intractable emulsion which not only proved very difficulty to clean from the condenser ~zz~
- ~ - A.420 suxface, but as it built up steadily reduced the efficacy of the condenser. One attempt to provide a process involving the use of a surface condenser which allegedly avoided the problems associated with the condensate emulsion is described in DE-A-29 38 805 which teaches condensing the steam and entrained materials at a temperature above 30C and relatively high pressures requiring higher energy input. An alternative approach to the problem is advocated in GB- A-l 080 057 which employs an indirect freezer condenser operating at a temperature between ~20 and -40C so that the condensate forms in the solid phase. In practice however we have found that in use each of these process~s as described gives rise to one or more problems.
According to the present invention there is provided a process for deodorising a triglyceride oil comprising passing dry steam throu~h the oil, the oil being at a temperature between 160C and 280C and under a pressure of between 0.1 to 8.0 mbar and condensing by indirect condenser means a vapour phase having a Reynolds number below 2300 and comprising steam, volatile materials from the oil and less than 100 mg neutral oil per m3 of steam when measured under the conditions prevailing in the headspace above the oil.
We have discovered that the combination of the use of dry steam, low headspace pressures in the range 0.1 to 8.0 mbax, preferably 0.1 to 4.0 mbar, more preferably 0.5 to
2.0 mbar, and the indirect condensation of a vapour phase having the stated Reynolds number and containing less than 100 mg, preferably less than 10 mg, neutral oil per m3 of steam when measured under the stated conditions yields a condensate which can be readily removed from the condenser surfaces. In paxticular, we have found that the formations of emulsions can be avoidedO
~l2;~
~l2;~
- 3 - A.420 By "dry" steam we mean a steam in which the equilibrium vapour pressure of pure water is more than the pressure under which the steam is maintained prior to passage through the oil.
As the steam passes through the oil it not only volatilises, as desired, volatile materials, but it can also entrain droplets of neutral oil. Preferably the oil is at a temperature between 180 and 270C. The stated level of oil required in the vapour to be condensed can be achieved in a number of ways. For example the low oil level can be achieved by separating entrained oil droplets from the vapour, for example, by employing a dem.ister and/or a pre-condenser. The pre-condenser is suitably a conventional vapour scrubber or water cooled heat exchanger and is arranged to operate in the temperature range of 20 to 150C, preferably 40 to 70C so as in addition to condense free fatty acids in the vapour.
Alternatively, or as well as, the velocity and pressure of steam can be controlled so that the amount of entrained oil in the vapour phase is reduced. To achieve a level of less than 10 mg oil per m steam of entrained oil, as measured in the headspace above the oil, the velocity of the steam (ms/A) is controlled to between about 1.7 and 16.0 kg per hour and square meter cross~sectional area of headspace of the deodoriser. The actual velocity selected will depend on the headspace pressure according to the formula:
ms/A ~ 5.5 I
where ~s = mass of steam per time unit (kg/h) P = head space pressure (mbar) A = cross sectional area deodoriser (m2) ~;~2'~
.
As the steam passes through the oil it not only volatilises, as desired, volatile materials, but it can also entrain droplets of neutral oil. Preferably the oil is at a temperature between 180 and 270C. The stated level of oil required in the vapour to be condensed can be achieved in a number of ways. For example the low oil level can be achieved by separating entrained oil droplets from the vapour, for example, by employing a dem.ister and/or a pre-condenser. The pre-condenser is suitably a conventional vapour scrubber or water cooled heat exchanger and is arranged to operate in the temperature range of 20 to 150C, preferably 40 to 70C so as in addition to condense free fatty acids in the vapour.
Alternatively, or as well as, the velocity and pressure of steam can be controlled so that the amount of entrained oil in the vapour phase is reduced. To achieve a level of less than 10 mg oil per m steam of entrained oil, as measured in the headspace above the oil, the velocity of the steam (ms/A) is controlled to between about 1.7 and 16.0 kg per hour and square meter cross~sectional area of headspace of the deodoriser. The actual velocity selected will depend on the headspace pressure according to the formula:
ms/A ~ 5.5 I
where ~s = mass of steam per time unit (kg/h) P = head space pressure (mbar) A = cross sectional area deodoriser (m2) ~;~2'~
.
- 4 - A.420 In practice a combination of means to separate entrained oil droplets and attention to steam velocity is preferably employed so that steam velocities in excess of 16.0 k~/hr can be employed pex m2 cross-sectional area of headspace of deodoriser. Preferred steam velocities can be up to a factor of 4 higher than that given by the above equation and can thus lie between between 16.8 and 64 kg/(hm2). The particular procedure selected in any case will depend on the system employed. For example higher pressures between 4.00 and 8.00 mbar can be be employed with a packed column deodoriser. In use the present process can employ a vapour phase having a neutral oil content down to 0.01 mg per m3 steam when measured under the conditions prevailing in the headspace above the oil.
The vapour phase can either be condensed to a liquid phase or a solid phase. In the former case the pressure of the vapour phase is preferably increased to above 10 mbar, but suitably from an economic point of view not more than about 60 mbar prior to entry into the condenser which is preferably operated at a temperatuxe between 0C and 25C and can be cooled by any suitable medium for example water. To increase the pressure of the vapour phase a mechanical pump is preferably employed. A mechanical pump is preferred over a conventional steam booster as it imparts less energy to the vapour and hence lessens the xisk that an emulsion may form. To condense the vapour phase directly to the solid phase a pressure of 0.1 to 8O0 mbar, preferably 0.1 to 4.0 mbar were preferably 0.5 to 2.0 mbar is suitably maintained in the condenser which is suitably operated at a temperature between -20 and -50C~
Suitable r~frigerants include N~3 and Freons.
In order to achieve a preferred rate of condensation of condensate in the ~ondenser means the flow path through the condenser means preferably has a crosscsectional area .
~2'~
The vapour phase can either be condensed to a liquid phase or a solid phase. In the former case the pressure of the vapour phase is preferably increased to above 10 mbar, but suitably from an economic point of view not more than about 60 mbar prior to entry into the condenser which is preferably operated at a temperatuxe between 0C and 25C and can be cooled by any suitable medium for example water. To increase the pressure of the vapour phase a mechanical pump is preferably employed. A mechanical pump is preferred over a conventional steam booster as it imparts less energy to the vapour and hence lessens the xisk that an emulsion may form. To condense the vapour phase directly to the solid phase a pressure of 0.1 to 8O0 mbar, preferably 0.1 to 4.0 mbar were preferably 0.5 to 2.0 mbar is suitably maintained in the condenser which is suitably operated at a temperature between -20 and -50C~
Suitable r~frigerants include N~3 and Freons.
In order to achieve a preferred rate of condensation of condensate in the ~ondenser means the flow path through the condenser means preferably has a crosscsectional area .
~2'~
- 5 - A.420 which at least in part decreases in the direction or flow of the vapour phase. The decrease in cross-sectional area of the flow path is preferably arranged so that the flow rate of the vapour phase through the condensex means is maintained substantially constant with respect to the cross-sectional area of the flow path. For any one case the flow path is thus preferably arranged such that the ~, Reynolds numbex of the vapour entering the flow path is substantially equal to the Reynolds number of the vapour phase leaving the flow path. Suitably the decrease is such that the ratio of the cross-sectional area of the inlet to the flow path to the cross-sectional area of the outlet to the flow path lies within the range of between 50:1 and 5:1. The decrease is preferable due to the deposition oE condensate as the vapour phase passes along the flow path. Due to the decrease deposition of each of the components of the vapour phase having condensation requirements with the temperature and pressure conditions of the flow path can be achieved such that the sole effluent from the flow path can be reduced to residual air and moisture only~ It can thus be possible to arrange for the effluent composition to be suitable for direct release into the atmosphere. The condenser means can be in one or more parts, for example it may be convenient to arrange the condenser means so that between 60 and 85 wt of the vapour phase condenses in a part with a relatively wide flow path and the remainder of the condensable material in the vapour phase condenses is a part with a relatively narrow flow path.
Advantageously where a pre-condenser is employed it can have a flow path whose cross-sectional area decreases in the direction of vapour flow. The degree of decreas~
is preferably arranged to maintain the ratio of condensable to non-condensable material in the pre-condenser substantially constant. Such an arrangement can be particularly advantageous where a large
Advantageously where a pre-condenser is employed it can have a flow path whose cross-sectional area decreases in the direction of vapour flow. The degree of decreas~
is preferably arranged to maintain the ratio of condensable to non-condensable material in the pre-condenser substantially constant. Such an arrangement can be particularly advantageous where a large
- 6 - A.420 amount of fatty acids are removed, for example, during distillative neutralisation and/or a headspace at the upper end of the stated range is employed, for example when using a packed column deodoriser.
5O1id condensate from the condenser can be removed by adjusting the temperature and/or pressure conditions.
Preferably the adjustment is such to liquidise the solid condensate which can then be drained from the condenser.
The adjustment preferably comprises admitting air at atmospheric pressure to the flow path. Collection and separation of the condensate into two or more portions may be performed to separate for example useful tocopherols from the remainder of the mixture~
Whether the condensate is collected in liquid or solid form, the flow path through the condenser is preferably tortuous. Increased heat and mass transfer and hence deposition of condensate can thus be obtained.
~0 Laminar flow ~ie Reynolds number <2300) is, however, maintained throughout the flow path. Preferably the Reynolds number of the vapour phase in the flow path is below lO00 and above lO. The flow path is preferably defined by inter alia tubular members of the condenser carrying the cooling medium. The tubular members are preferably finned and can be separated by one or more baffles.
The present process can be operated as a batch process, a semi-continuous process or a continuous process. Where the condensate is in liquid form it can be continuously drained from the condenser. As in the case of a solid condensate the collected condensate can be separated into two or more por$ions to separate for example useful tocopherols from the remainder of the condensate mixture. ~e have found that the present condensate whether collected in liquid or solid form readily allows separation into two or more portions or phases.
5O1id condensate from the condenser can be removed by adjusting the temperature and/or pressure conditions.
Preferably the adjustment is such to liquidise the solid condensate which can then be drained from the condenser.
The adjustment preferably comprises admitting air at atmospheric pressure to the flow path. Collection and separation of the condensate into two or more portions may be performed to separate for example useful tocopherols from the remainder of the mixture~
Whether the condensate is collected in liquid or solid form, the flow path through the condenser is preferably tortuous. Increased heat and mass transfer and hence deposition of condensate can thus be obtained.
~0 Laminar flow ~ie Reynolds number <2300) is, however, maintained throughout the flow path. Preferably the Reynolds number of the vapour phase in the flow path is below lO00 and above lO. The flow path is preferably defined by inter alia tubular members of the condenser carrying the cooling medium. The tubular members are preferably finned and can be separated by one or more baffles.
The present process can be operated as a batch process, a semi-continuous process or a continuous process. Where the condensate is in liquid form it can be continuously drained from the condenser. As in the case of a solid condensate the collected condensate can be separated into two or more por$ions to separate for example useful tocopherols from the remainder of the condensate mixture. ~e have found that the present condensate whether collected in liquid or solid form readily allows separation into two or more portions or phases.
- 7 - A.420 When operating a batch process the adjustment of the condenser to liquidate solid condensate can conveniently take place whilst treated oil is being emptied from and/or further oil being filled into the batch vessel. In such S an arrangement only one condenser need thus he required.
Such an arrangement is advantageous in that only valve means need be provided to separate the condenser from the batch vessel, but no junction point is necessary at the inlet to the condenser. When operating a continuous or semi-continuous process with solid condensate collection more than one condenser is preferably present. Valve means to vary the condenser in use is preferably installed so that the condenser in use can be altered to allow intermittent removal of the solid condensate from any 5 other condenser present.
According to a second aspect of the present invention there is provided apparatus for deodorising a triglyceride oil comprising heating means to heat in use oil to a temperature between 160 and 280C, means for maintaining in use a pressure above the oil of between 0.1 and 8.0 mbar, preferably between 0.1 and 4.0 mbar, more preferably between 0.5 and 2.0 mbar, means for passing in use dry steam through the oil and indirect condenser means having a flow path arranged to receive a vapour phase having a Reynolds number less than 2300 and comprising steam, volatile materials from the oil and less than lOOmg neutral oil per m of steam when measured under the conditions prevailing in the headspace above the oil.
Preferably the flow path has at least in part a cross-sectional area which decreases in the direction of flow of the vapour phase, The rate of decre;~se of the cross-sectional area of the flow path is preferably such that the ratio of the
Such an arrangement is advantageous in that only valve means need be provided to separate the condenser from the batch vessel, but no junction point is necessary at the inlet to the condenser. When operating a continuous or semi-continuous process with solid condensate collection more than one condenser is preferably present. Valve means to vary the condenser in use is preferably installed so that the condenser in use can be altered to allow intermittent removal of the solid condensate from any 5 other condenser present.
According to a second aspect of the present invention there is provided apparatus for deodorising a triglyceride oil comprising heating means to heat in use oil to a temperature between 160 and 280C, means for maintaining in use a pressure above the oil of between 0.1 and 8.0 mbar, preferably between 0.1 and 4.0 mbar, more preferably between 0.5 and 2.0 mbar, means for passing in use dry steam through the oil and indirect condenser means having a flow path arranged to receive a vapour phase having a Reynolds number less than 2300 and comprising steam, volatile materials from the oil and less than lOOmg neutral oil per m of steam when measured under the conditions prevailing in the headspace above the oil.
Preferably the flow path has at least in part a cross-sectional area which decreases in the direction of flow of the vapour phase, The rate of decre;~se of the cross-sectional area of the flow path is preferably such that the ratio of the
- 8 - A.420 cross-sectional area of the inlet to the cross-sectional area of the outlet to the flow path lies within the range of from 50:1 to 5:1. The rate of decrease selected in any one case will be determined inter alia by the ratio of condensable to non-condensable material in the vapour phase and heat and mass transfer characteristics of the vapour phase. Suitably the decrease is such that the Reynolds number of the vapour phase at the inlet is substantially equal to the Reynolds number of the vapour phase at the outlet.
The temperature and pressure conditions in the flow path of the condenser means ar~ selected appropriately.
Preferably the condenser means is adapted to maintain in use conditions of pressure and temperature in the flow path of between 0.1 and 8.0 mbar, preferably between 0.1 and 4.0 mbar, more preferably 0.5 and 2.0 mbar, and between -50 and -20C~ Such ambient temperature in the flow path can be provided by any suitable refrigerant such as for example ammonia, fluorocarbons and chlorocarbons.
In the case of flow path conditions arranged to achieve solid condensate pump means to provide the necessary vacuum conditions are suitably located after the condenser means. Any pump means can be employed provided it provides the required pressure~ An example of a suitable pump means is a rotary vane pump.
Preferably the condenser means is adapted to maintain pressure and temperature conditions in the flow path of between 10 mbar and ~0 mbar and 0C and 25C~ Suitable cooling agent is water. Suitable pump means is for example mechanical pump is located before the condenser means~
Preferably the flow path is tortuous. The tortuosity is preferably provided by tubular members of lZ244 ~ 9 - g - A.420 the condenser which are preferably finned. ~affles may also be provided in the condenser.
Preferably the apparatus includes a second condenser means adapted for, in use, passage of the vapour phase therethrough prior to passage through the first said condenser means, the second condenser'means being for, in usP, condensation of fatty acids in liquid form. The second condenser means can for example be a conventional vapour scrubber or water cooled heat exchanger. If required a demister can be included in the apparatus.
Preferably, the apparatus includes valve means adapted to close the entrance to the flow path.
Additionally the apparatus preferably includes means adapted to adjust the ambient temperature and/or pressure in the flow path so as in use to liquidise solid condensate and remove it. The apparatus can moreover include means to separate into one or more portions condensate formed in the first condenser means~
If desired the apparatus can include a plurality of the irst said condenser means and means to direct, in use, the vapour phase to any one of the said plurality.
Variation of the first condenser means in use can thus allow removal of the solid condensate from one condenser means without the necessity to close down the treatment process.
The present invention is applicable to the treatment of any triglyceride oil which requires deodorisation treatment, optionally in combination with distillative deacidification. Examples of such oils are soyabean oil, sunflower oil, palm oil, rapeseed oil, coconut oil, fish oil tallow, mixtures and fractions thereof. Particularly coconut oil and soyabean oil can be subjected to - 10 - A.420 distillative deacidification by the present process and apparatus.
It it to be understood that the present invention extends to the products of the present process and to oils treated by the present apparatus.
i An embodiment of the present invention by way of example only will now be described with reference to the 10 accompanying drawings; wherein: ¦
Fig. 1 shows in diagrammatic form a form of apparatus embodying the present invention;
Fig. 2 is a vertical elevation ~iew of the inside of condenser 14, of Fig. l; and 15Fig.3 is a horizontal cross-section along the line a-a in Fig. 2.
Referring firstly to Fig. 1 the apparatus includes a deodoriser chamber 10 having an inlet for steam and an outlet for volatile materials. Exit and entry means are also provided for oil. The outlet leads to a vapour cooler 12 which in the present embodiment is a vapour - scrubber. An outlet from the vapour cooler 12 leads to the condenser 14. An outlet from the condenser 14 leads to a vacuum pump 16 which in use is able to produce a pressure of from 0.5 to 2 mbar throughout the apparatus~
The vacuum pump is a mechanical rotary vane pump.
The interior construction of the condenser 14 is described with reference to Figs. 2 and 3. The condenser 14 has at one lateral end face an inlet 16 and at an opposite and narrower lateral end face an outlet 18 Between the inlet 16 and the outlet 18 are arranged a plurality of tubes 20 extending the height of the ~ondenser 14 and arranged in rows trans~erse to the two said end faces. Each of the tubes 20 is finned !
~2~ g ~ A.420 longitudinally~ The arrangement of the rows of the tubes and of the finning on the tubes is chosen so as to achieve laminar flow conditions. Each tube carries a heat exchange medium which, depending on use is liquid ammonia or water. With respect to each row of tubes 20 the fins 22 extend alternately from the ceiling and the floor of the condenser 14, in each case stopping short of the floor and ceiling respectively as shown in Fig. 2. Each row of tubes 20 is separated from its neighbour or neighbours by respective fixed vertical baffles 24 which extend alternately from the ceiling and the floor and, as shown in Fig. 2, stop short of the floor and ceiling respectively. The finned tubes 20 and the baffles 24 thus define a tortuous path 26 from the inlet 16 to the outlet 18.
The cross sectional diameter of the tubes 20 and the spacing between adjacent tubes and between neighbouring rows decreases on passing from the inlet 16 to the outlet 18. Suitably the spacing between nearest points of adjacent finned tubes at the inlet end of the flow path is about 100 mm and between adjacent tubes at the ol~tlet end of the flow path about 10 mm or as close as possible.
The dimensions of the end faces, tube spacings and dimensions are selected so that the cross sectional area of the tortuous flow path 26 decreases on passing from the inlet 16 to the outlet 18. The ratio of the cross sectional area of the inlet to the cross-sectional area of the outlet of the flow path is 20:1~ The change in cross-sectional area is selected so that the heat transfer co-efficient between the medium passing through the condenser and the surface of the finned tubes 20 remains substantially uniform as material is condensed in the condenser~ ie so tht the R~ynolds number of the vapour phase at the inlet is substantially e~ual to the Reynolds number of the vapour phase at the outlet.
- 12 - A.420 In operation the deodoriser chamber is filled with oil to be treated. The chamber is evacuated to 0.5 to 2.0 mbar and the oil heated to the desired temperature.
Super-heated steam is fed into the oil. The resulting vapour phase having a pressure of from 0.5 to 2.0 mbar and comprising steam, volatile materials entrained by the steam on its passage through the oil passes to the vapour coolex 12 which is maintained at a temperature between 50 and 60C. In the vapour cooler fatty acids and other components of similar low volatility contained in the vapour phase condense to a li~uid. The remaining vapour phase passes to condenser 14 and enters the flow path 26.
The condenser, when using ammonia, is maintained at a temperature of between -50 and -20C. The pump maintains a pressure throughout the apparatus including the condenser within the range of from 0.5 to 2.0 mbar. The sole effluent to the atmosphere comprises air, arising from unavoidable leaks into the apparatus, and a small amount of moistureO
In an alternative embodiment the vapour cooler 12 is omitted. In operation the vapour phase comprising steam, volatile materials passed directly from the deodoriser chamber 10 to the condenser 14.
Examples of use of the alternative embodiment of apparatus with the vapour cooler 12 omitted will now be described:
Exa~ s l to 12 Examples 1 to 12 were performed with the following oils:
- 13 - A.420 1. A mixture of neutralised and bleached soyabean oil and hardened soyabean oil having an overall free fatty acid content of about 0~1 wt%.
2. Distillative neutralisation of soyabean oil 3. Neutralised and bleached rapeseed oil 4. Distillative neutralisation of rapeseed oil containing 0.87 wt% free fatty acid 5. Neutralised and bleached sunflower oil 6. Distillative neutralisation of sunflower oil 7. Palm oil 8. Palm olein
The temperature and pressure conditions in the flow path of the condenser means ar~ selected appropriately.
Preferably the condenser means is adapted to maintain in use conditions of pressure and temperature in the flow path of between 0.1 and 8.0 mbar, preferably between 0.1 and 4.0 mbar, more preferably 0.5 and 2.0 mbar, and between -50 and -20C~ Such ambient temperature in the flow path can be provided by any suitable refrigerant such as for example ammonia, fluorocarbons and chlorocarbons.
In the case of flow path conditions arranged to achieve solid condensate pump means to provide the necessary vacuum conditions are suitably located after the condenser means. Any pump means can be employed provided it provides the required pressure~ An example of a suitable pump means is a rotary vane pump.
Preferably the condenser means is adapted to maintain pressure and temperature conditions in the flow path of between 10 mbar and ~0 mbar and 0C and 25C~ Suitable cooling agent is water. Suitable pump means is for example mechanical pump is located before the condenser means~
Preferably the flow path is tortuous. The tortuosity is preferably provided by tubular members of lZ244 ~ 9 - g - A.420 the condenser which are preferably finned. ~affles may also be provided in the condenser.
Preferably the apparatus includes a second condenser means adapted for, in use, passage of the vapour phase therethrough prior to passage through the first said condenser means, the second condenser'means being for, in usP, condensation of fatty acids in liquid form. The second condenser means can for example be a conventional vapour scrubber or water cooled heat exchanger. If required a demister can be included in the apparatus.
Preferably, the apparatus includes valve means adapted to close the entrance to the flow path.
Additionally the apparatus preferably includes means adapted to adjust the ambient temperature and/or pressure in the flow path so as in use to liquidise solid condensate and remove it. The apparatus can moreover include means to separate into one or more portions condensate formed in the first condenser means~
If desired the apparatus can include a plurality of the irst said condenser means and means to direct, in use, the vapour phase to any one of the said plurality.
Variation of the first condenser means in use can thus allow removal of the solid condensate from one condenser means without the necessity to close down the treatment process.
The present invention is applicable to the treatment of any triglyceride oil which requires deodorisation treatment, optionally in combination with distillative deacidification. Examples of such oils are soyabean oil, sunflower oil, palm oil, rapeseed oil, coconut oil, fish oil tallow, mixtures and fractions thereof. Particularly coconut oil and soyabean oil can be subjected to - 10 - A.420 distillative deacidification by the present process and apparatus.
It it to be understood that the present invention extends to the products of the present process and to oils treated by the present apparatus.
i An embodiment of the present invention by way of example only will now be described with reference to the 10 accompanying drawings; wherein: ¦
Fig. 1 shows in diagrammatic form a form of apparatus embodying the present invention;
Fig. 2 is a vertical elevation ~iew of the inside of condenser 14, of Fig. l; and 15Fig.3 is a horizontal cross-section along the line a-a in Fig. 2.
Referring firstly to Fig. 1 the apparatus includes a deodoriser chamber 10 having an inlet for steam and an outlet for volatile materials. Exit and entry means are also provided for oil. The outlet leads to a vapour cooler 12 which in the present embodiment is a vapour - scrubber. An outlet from the vapour cooler 12 leads to the condenser 14. An outlet from the condenser 14 leads to a vacuum pump 16 which in use is able to produce a pressure of from 0.5 to 2 mbar throughout the apparatus~
The vacuum pump is a mechanical rotary vane pump.
The interior construction of the condenser 14 is described with reference to Figs. 2 and 3. The condenser 14 has at one lateral end face an inlet 16 and at an opposite and narrower lateral end face an outlet 18 Between the inlet 16 and the outlet 18 are arranged a plurality of tubes 20 extending the height of the ~ondenser 14 and arranged in rows trans~erse to the two said end faces. Each of the tubes 20 is finned !
~2~ g ~ A.420 longitudinally~ The arrangement of the rows of the tubes and of the finning on the tubes is chosen so as to achieve laminar flow conditions. Each tube carries a heat exchange medium which, depending on use is liquid ammonia or water. With respect to each row of tubes 20 the fins 22 extend alternately from the ceiling and the floor of the condenser 14, in each case stopping short of the floor and ceiling respectively as shown in Fig. 2. Each row of tubes 20 is separated from its neighbour or neighbours by respective fixed vertical baffles 24 which extend alternately from the ceiling and the floor and, as shown in Fig. 2, stop short of the floor and ceiling respectively. The finned tubes 20 and the baffles 24 thus define a tortuous path 26 from the inlet 16 to the outlet 18.
The cross sectional diameter of the tubes 20 and the spacing between adjacent tubes and between neighbouring rows decreases on passing from the inlet 16 to the outlet 18. Suitably the spacing between nearest points of adjacent finned tubes at the inlet end of the flow path is about 100 mm and between adjacent tubes at the ol~tlet end of the flow path about 10 mm or as close as possible.
The dimensions of the end faces, tube spacings and dimensions are selected so that the cross sectional area of the tortuous flow path 26 decreases on passing from the inlet 16 to the outlet 18. The ratio of the cross sectional area of the inlet to the cross-sectional area of the outlet of the flow path is 20:1~ The change in cross-sectional area is selected so that the heat transfer co-efficient between the medium passing through the condenser and the surface of the finned tubes 20 remains substantially uniform as material is condensed in the condenser~ ie so tht the R~ynolds number of the vapour phase at the inlet is substantially e~ual to the Reynolds number of the vapour phase at the outlet.
- 12 - A.420 In operation the deodoriser chamber is filled with oil to be treated. The chamber is evacuated to 0.5 to 2.0 mbar and the oil heated to the desired temperature.
Super-heated steam is fed into the oil. The resulting vapour phase having a pressure of from 0.5 to 2.0 mbar and comprising steam, volatile materials entrained by the steam on its passage through the oil passes to the vapour coolex 12 which is maintained at a temperature between 50 and 60C. In the vapour cooler fatty acids and other components of similar low volatility contained in the vapour phase condense to a li~uid. The remaining vapour phase passes to condenser 14 and enters the flow path 26.
The condenser, when using ammonia, is maintained at a temperature of between -50 and -20C. The pump maintains a pressure throughout the apparatus including the condenser within the range of from 0.5 to 2.0 mbar. The sole effluent to the atmosphere comprises air, arising from unavoidable leaks into the apparatus, and a small amount of moistureO
In an alternative embodiment the vapour cooler 12 is omitted. In operation the vapour phase comprising steam, volatile materials passed directly from the deodoriser chamber 10 to the condenser 14.
Examples of use of the alternative embodiment of apparatus with the vapour cooler 12 omitted will now be described:
Exa~ s l to 12 Examples 1 to 12 were performed with the following oils:
- 13 - A.420 1. A mixture of neutralised and bleached soyabean oil and hardened soyabean oil having an overall free fatty acid content of about 0~1 wt%.
2. Distillative neutralisation of soyabean oil 3. Neutralised and bleached rapeseed oil 4. Distillative neutralisation of rapeseed oil containing 0.87 wt% free fatty acid 5. Neutralised and bleached sunflower oil 6. Distillative neutralisation of sunflower oil 7. Palm oil 8. Palm olein
9. Fish oil lO. Tallow olein ll. Neutralised and bleached coconut oil 12. Distillative neutralisation of cxude coconut oil containing 2.1 wt~ free fatky acid A 300 kg batch of oil was placed in the deodoriser chamber 10. Temperature and pressure conditions prevailing in the chamber 13 were adjusted to between 190 and 240C and 1.0 to 1.5 mbar xespectively~ Dry steam at a constant flow rate with ~s between 1.2 and 2~0 kg/h was fed to the deodoriser chamber~ The resulting vapour phase was led through the condenser 14. In the condenser 14 the vapour phase was maintained at a pressure of 1.0 ~22~8~
- 14 - A.420 mbar or less and a temperature of -30C with a cooling medium of the condenser 14 at a temperature between -40 and -50C. In the condenser 14 the Reynolds number of the vapour phase lay between 400 and 600.
On completion of tha deodorisation air was admitted to the condenser 14 and the condenser was indirectly heated to 60C. At 60C the solid deposits formed were liquid which in each case readily drained from the condenser. The liquid was a two phase mixture. It was not however in the form of an emulsion. On average at least 95 wt% of the steam injected into the oil was recovered as water in the condenser 14. The oily phase of the condensate included, depending on the oil, a mixture of inter alia tocopherols and free fatty acids.
A free draining liquid was obtained on heating, however, even in the case of distillative neutralisation such as Example 12 in which the condensatPs contained 6.4 kg freQ
fatty acid. In each case the neutral oil loss was less than 30g which repxesented a neutral oil content in the vapour phase when measured under the conditions prevailing in the headspace in the deodoriser chamber above the oil of less than 10 mg per m3 steam.
.
Comparative ~xamples A & B
A. Bleached but unneutralised soyabean oil was subj@cted to distillative neutralisation under the above conditions but with the exception that wet steam was employed. 2kg of condensate was formed in sondenser 14. On heating the condenser 14 the condensate was found to be in the form of an emulsion which was difficult to remove from condenser 1~ .
B. The same oil and conditions were employed as in Comparative Example A with the exception that dry steam .
~2~
15 - ~.420 was employed but at a throughput rate of 6 kg/h. The high flow rate increased the neutral oil content to about 800 g/h which gave rise to a neutral oil content in the vapour phase entering the condenser 14 of about 120 mg per m3 steam as measured under the conditions prevailing in the headspace of the deodoriser chamber 10. On I
heating the condenser 14 the condensate was found to be 1, in the form of an emulsion which could not be readily removed from the condenser 140 , Example 13 The present example illustrates the use of the present process and apparatus to form a liquid condensate direct. Usiny an embodiment in which the vapour cooler is omitted and a mechanical vacuum pump is located intermediate the deodoriser chamber 10 and condenser 14, 300 kg neutralised and bleached soyabean oil are deodorised at a temperature of 240C and a pressure of 2.0 mbar dry steam being passed through the chamber 10 at a constant rate of 2.0 kg/h. The resulting phase is fed through the mechanical pump to increase the pressure to 42 mbar. The vapour phase has a Reynolds numher of about 500 and is led into the condenser 14 which is cooled with water at a temperature of about 20C. The liquid condensate comprising a mixture of water and fatty material not in the form of the emulsion could be readily pumped away. The neutral oil content in the vapour phase is less than 10 mg per m3 steam as measured in the conditions in the deodoriser chamber headspace.
- 14 - A.420 mbar or less and a temperature of -30C with a cooling medium of the condenser 14 at a temperature between -40 and -50C. In the condenser 14 the Reynolds number of the vapour phase lay between 400 and 600.
On completion of tha deodorisation air was admitted to the condenser 14 and the condenser was indirectly heated to 60C. At 60C the solid deposits formed were liquid which in each case readily drained from the condenser. The liquid was a two phase mixture. It was not however in the form of an emulsion. On average at least 95 wt% of the steam injected into the oil was recovered as water in the condenser 14. The oily phase of the condensate included, depending on the oil, a mixture of inter alia tocopherols and free fatty acids.
A free draining liquid was obtained on heating, however, even in the case of distillative neutralisation such as Example 12 in which the condensatPs contained 6.4 kg freQ
fatty acid. In each case the neutral oil loss was less than 30g which repxesented a neutral oil content in the vapour phase when measured under the conditions prevailing in the headspace in the deodoriser chamber above the oil of less than 10 mg per m3 steam.
.
Comparative ~xamples A & B
A. Bleached but unneutralised soyabean oil was subj@cted to distillative neutralisation under the above conditions but with the exception that wet steam was employed. 2kg of condensate was formed in sondenser 14. On heating the condenser 14 the condensate was found to be in the form of an emulsion which was difficult to remove from condenser 1~ .
B. The same oil and conditions were employed as in Comparative Example A with the exception that dry steam .
~2~
15 - ~.420 was employed but at a throughput rate of 6 kg/h. The high flow rate increased the neutral oil content to about 800 g/h which gave rise to a neutral oil content in the vapour phase entering the condenser 14 of about 120 mg per m3 steam as measured under the conditions prevailing in the headspace of the deodoriser chamber 10. On I
heating the condenser 14 the condensate was found to be 1, in the form of an emulsion which could not be readily removed from the condenser 140 , Example 13 The present example illustrates the use of the present process and apparatus to form a liquid condensate direct. Usiny an embodiment in which the vapour cooler is omitted and a mechanical vacuum pump is located intermediate the deodoriser chamber 10 and condenser 14, 300 kg neutralised and bleached soyabean oil are deodorised at a temperature of 240C and a pressure of 2.0 mbar dry steam being passed through the chamber 10 at a constant rate of 2.0 kg/h. The resulting phase is fed through the mechanical pump to increase the pressure to 42 mbar. The vapour phase has a Reynolds numher of about 500 and is led into the condenser 14 which is cooled with water at a temperature of about 20C. The liquid condensate comprising a mixture of water and fatty material not in the form of the emulsion could be readily pumped away. The neutral oil content in the vapour phase is less than 10 mg per m3 steam as measured in the conditions in the deodoriser chamber headspace.
Claims (24)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. Process for deodorising a triglyceride oil comprising passing dry steam through the oil, the oil being at a temperature between 160°C and 280°C and under a pressure of between 0.1 to 8.0 mbar and condensing by indirect condenser means a vapour phase having a Reynolds number less than 2300 and comprising steam, volatile materials from the oil and less than 100 mg neutral oil per m3 of steam when measured under the conditions prevailing in the headspace above the oil.
2. Process according to Claim 1 wherein the oil is under a pressure of between 0.5 and 2.0 mbar.
3. Process according to Claim 1 wherein the vapour phase has a Reynolds number of less than 1000.
4. Process according to Claim 1 wherein the velocity of steam lies between 1.7 and 16.0 kg/hr per m2 cross-sectional area of headspace above the oil.
5. Process according to Claim 1 wherein entrained oil droplets are removed from the vapour phase prior to entry in the indirect condenser.
6. Process according to Claim 5 wherein a demister means is employed.
7. Process according to Claim 1 employing a pre-condenser means arranged to remove fatty acids present in the vapour phase.
8. Process according to Claim 6 or Claim 7 wherein the velocity of steam passed through the oil lies between 6.8 and 64 kg/hr per m2 cross-sectional area of headspace above the oil.
9. Process according to Claim 1 including draining condensate from the condenser.
10. Process according to Claim 9 including separating the drained condensate into at least two portions.
11. Process according to Claim 1 wherein the condenser has a tortuous path.
12. Process according to Claim 1 wherein the vapour phase is condensed in the indirect condenser to a liquid phase.
13. Process according to Claim 12 wherein the pressure of the vapour phase is increased to between 10 mbar and 60 mbar by means of a mechanical pump prior to entry into the condenser.
14. Process according to Claim 1 wherein the vapour phase is condensed in the indirect condenser to a solid phase.
15. Process according to Claim 14 wherein the temperature and pressure conditions in the condenser range from -50 to -20°C and 0.1 to 8.0 mbar respectively.
16. Process according to Claim 1 wherein the flow path through the condenser has a cross-sectional area which at least in part of the flow path decreases in the direction of flow of the vapour phase.
17. Process according to Claim 16 wherein the decrease is such that the ratio of the cross-sectional area of the inlet to the flow path to the cross-sectional area of the outlet of the flow path lies within the range of between 50:1 and 5:1.
18. Apparatus for deodorising a triglyceride oil comprising heating means to heat in use oil to a temperature between 160 and 280°C, means for maintaining in use a pressure above the oil of between 0.1 and 8.0 mbar, means for passing in use dry steam through the oil and indirect condenser means having a flow path arranged to receive a vapour phase having a Reynolds number less than 2300 and comprising steam, volatile materials from the oil, and less than 100mg neutral oil per m3 of steam when measured under the conditions prevailing in the headspace above the oil.
19. Apparatus according to Claim 18 wherein the flow path of the condenser means has at least in part a cross-sectional area which descreases in the direction of flow of the vapour phase.
20. Apparatus according to Claim 19 wherein the rate of decrease of the cross-sectional area of the flow path is such that the ratio of the cross-sectional area of the inlet of the flow path to the cross-sectional area of the outlet of the flow path lies within the range of from 50:1 to 5:1.
21. Apparatus according to Claim 18 wherein the flow path is tortuous.
22. Apparatus according to Claim 18 including a second condenser means adapted for, in use, passage of the vapour phase therethrough prior to passage through the first said condenser means and for, in use, condensing in liquid form fatty acids from the vapour phase.
23. Apparatus according to Claim 18 wherein the first condenser means is adapted to maintain pressure and temperature conditions in the flow path, in use, of between 0.1 and 8.0 mbar and between -50 and -20°C.
24. Apparatus according to Claim 18 wherein the first condenser means is adapted in the flow path, in use, of between 10 and 60 mbar and 0 and 25°C.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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GB8314496 | 1983-05-25 | ||
GB838314496A GB8314496D0 (en) | 1983-05-25 | 1983-05-25 | Treating triglyceride oil |
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CA1224489A true CA1224489A (en) | 1987-07-21 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA000454958A Expired CA1224489A (en) | 1983-05-25 | 1984-05-23 | Deodorisation process for triglyceride oil |
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EP (1) | EP0127982B1 (en) |
JP (1) | JPS6058499A (en) |
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US4378317A (en) * | 1980-01-10 | 1983-03-29 | The Procter & Gamble Company | Process to maintain bland taste in energy efficient oil deodorization systems |
US4406836A (en) * | 1981-12-03 | 1983-09-27 | The Badger Company, Inc. | Method for condensing fatty acids |
FR2523465B1 (en) * | 1982-03-22 | 1988-04-01 | Alsthom Atlantique | DEVICE FOR SUCTION AND TREATMENT OF GAS, ESPECIALLY GAS FROM THE DEODORIZATION OF FATTY BODIES |
US4601790A (en) * | 1982-07-23 | 1986-07-22 | Hermann Stage | Process for deodorizing and/or physical refining of cocoa butter and cocoa butter substitutes |
DE3227669C1 (en) * | 1982-07-23 | 1983-07-07 | Hermann Dr. 4400 Münster Stage | Process and plant for deodorising and / or deacidifying edible oils, fats and esters |
-
1983
- 1983-05-25 GB GB838314496A patent/GB8314496D0/en active Pending
-
1984
- 1984-05-21 ZA ZA843826A patent/ZA843826B/en unknown
- 1984-05-22 AU AU28487/84A patent/AU563380B2/en not_active Ceased
- 1984-05-23 DE DE8484303491T patent/DE3473297D1/en not_active Expired
- 1984-05-23 CA CA000454958A patent/CA1224489A/en not_active Expired
- 1984-05-23 EP EP84303491A patent/EP0127982B1/en not_active Expired
- 1984-05-23 AT AT84303491T patent/ATE36346T1/en not_active IP Right Cessation
- 1984-05-25 JP JP59106300A patent/JPS6058499A/en active Pending
-
1987
- 1987-11-13 US US07/122,548 patent/US4838997A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
ATE36346T1 (en) | 1988-08-15 |
AU563380B2 (en) | 1987-07-09 |
ZA843826B (en) | 1986-01-29 |
US4838997A (en) | 1989-06-13 |
JPS6058499A (en) | 1985-04-04 |
DE3473297D1 (en) | 1988-09-15 |
EP0127982B1 (en) | 1988-08-10 |
AU2848784A (en) | 1984-11-29 |
GB8314496D0 (en) | 1983-06-29 |
EP0127982A1 (en) | 1984-12-12 |
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MKEX | Expiry |